GTR Home > Laboratories > Genetics Laboratory, Peroxisomal Disorders Section

Genetics Laboratory, Peroxisomal Disorders Section

GTR Lab ID: 1003, Last updated:2016-04-21


Conditions and tests

  • Adrenoleukodystrophy3 tests
  • Alpha-methylacyl-CoA racemase deficiency1 test
  • Bifunctional peroxisomal enzyme deficiency3 tests
  • Peroxisome biogenesis disorders, Zellweger syndrome spectrum9 tests
  • Phytanic acid storage disease2 tests
  • Pseudoneonatal adrenoleukodystrophy2 tests
  • Pyridoxine-dependent epilepsy1 test
  • Refsum disease, adult, 11 test
  • Rhizomelic chondrodysplasia punctata type 14 tests
  • Rhizomelic chondrodysplasia punctata type 22 tests
  • Rhizomelic chondrodysplasia punctata type 32 tests

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously

List of certifications/licenses


  • CLIAHelp, Number: 21D0649789, Expiration date: 2015-11-30
  • CAP, Number: 1353022, Expiration date: 2015-09-14


  • MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 802, Expiration date: 2015-06-30
  • PA - Pennsylvania Department of Health PADOH, Number: 033873, Expiration date: 2015-08-15

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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